MEDIMOD(TM), MODEL 8900— 510(k) K890705

Substantially Equivalent

Medical Devices, Inc.

FDA 510(k) clearance K890705 for MEDIMOD(TM), MODEL 8900, Substantially Equivalent on 1989-03-09. Applicant: Medical Devices, Inc.. Device class: 2.

Clearance details

Applicant: Medical Devices, Inc.
Product code: Code GZJ
Device class: Class 2
Regulation: 21 CFR 882.5890
Advisory panel: Neurology
Date received: 1989-02-10
Decision date: 1989-03-09
Decision: Substantially Equivalent
Clearance type: Traditional
Location: St. Paul, MN, US

Download summary PDF View on FDA.gov ↗

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Data sourced from openFDA. This site is unofficial and independent of the FDA.